TY - JOUR KW - Amino Acid Sequence KW - Animals KW - Base Sequence KW - Conserved Sequence KW - Drug Resistance, Microbial KW - Genes, Bacterial KW - Humans KW - leprosy KW - Mice KW - Molecular Sequence Data KW - Mutation KW - Mycobacterium leprae KW - Rifampin AU - Honoré N AU - Cole S T AB -

Rifampin is currently the most potent drug used in leprosy control programs. We show that the rifampin resistance which emerged in nine patients with lepromatous leprosy, who had received rifampin monotherapy, stemmed from mutations in the rpoB gene, which encodes the beta subunit of RNA polymerase of Mycobacterium leprae. In eight cases missense mutations were found to affect a serine residue, Ser-425, while in the remaining mutant a small insertion was found close to this site. These findings will be of use for the development of a rapid screening procedure, involving the polymerase chain reaction, for monitoring the emergence of rifampin-resistant M. leprae strains.

BT - Antimicrobial agents and chemotherapy C1 - http://www.ncbi.nlm.nih.gov/pubmed/8460911?dopt=Abstract DA - 1993 Mar DO - 10.1128/aac.37.3.414 IS - 3 J2 - Antimicrob. Agents Chemother. LA - eng N2 -

Rifampin is currently the most potent drug used in leprosy control programs. We show that the rifampin resistance which emerged in nine patients with lepromatous leprosy, who had received rifampin monotherapy, stemmed from mutations in the rpoB gene, which encodes the beta subunit of RNA polymerase of Mycobacterium leprae. In eight cases missense mutations were found to affect a serine residue, Ser-425, while in the remaining mutant a small insertion was found close to this site. These findings will be of use for the development of a rapid screening procedure, involving the polymerase chain reaction, for monitoring the emergence of rifampin-resistant M. leprae strains.

PY - 1993 SP - 414 EP - 8 T2 - Antimicrobial agents and chemotherapy TI - Molecular basis of rifampin resistance in Mycobacterium leprae. VL - 37 SN - 0066-4804 ER -